Asymmetric arrangement of two alpha subunits within Escherichia coli RNA polymerase Involvement of one alpha subunit in contact with cAMP receptor protein

1994 ◽  
Vol 236 (5) ◽  
pp. 1283-1288 ◽  
Author(s):  
Chao Zou ◽  
Nobuyuki Fujita ◽  
Akira Ishihama
1999 ◽  
Vol 337 (3) ◽  
pp. 415-423 ◽  
Author(s):  
Emma C. LAW ◽  
Nigel J. SAVERY ◽  
Stephen J. W. BUSBY

The Escherichia coli cAMP receptor protein (CRP) is a factor that activates transcription at over 100 target promoters. At Class I CRP-dependent promoters, CRP binds immediately upstream of RNA polymerase and activates transcription by making direct contacts with the C-terminal domain of the RNA polymerase α subunit (αCTD). Since αCTD is also known to interact with DNA sequence elements (known as UP elements), we have constructed a series of semi-synthetic Class I CRP-dependent promoters, carrying both a consensus DNA-binding site for CRP and a UP element at different positions. We previously showed that, at these promoters, the CRP–αCTD interaction and the CRP–UP element interaction contribute independently and additively to transcription initiation. In this study, we show that the two halves of the UP element can function independently, and that, in the presence of the UP element, the best location for the DNA site for CRP is position -69.5. This suggests that, at Class I CRP-dependent promoters where the DNA site for CRP is located at position -61.5, the two αCTDs of RNA polymerase are not optimally positioned. Two experiments to test this hypothesis are presented.


2005 ◽  
Vol 102 (49) ◽  
pp. 17693-17698 ◽  
Author(s):  
D. C. Grainger ◽  
D. Hurd ◽  
M. Harrison ◽  
J. Holdstock ◽  
S. J. W. Busby

1992 ◽  
Vol 6 (18) ◽  
pp. 2599-2605 ◽  
Author(s):  
Chao Zou ◽  
Nobuyuki Fujita ◽  
Kazuhiko Igarashi ◽  
Akira Ishihama

1998 ◽  
Vol 330 (1) ◽  
pp. 413-420 ◽  
Author(s):  
S. Georgina LLOYD ◽  
J. W. Stephen BUSBY ◽  
J. Nigel SAVERY

During transcription initiation at bacterial promoters, the C-terminal domain of the RNA polymerase α subunit (αCTD) can interact with DNA-sequence elements (known as UP elements) and with activator proteins. We have constructed a series of semi-synthetic promoters carrying both an UP element and a consensus DNA-binding site for the Escherichia coli cAMP receptor protein (CRP; a factor that activates transcription by making direct contacts with αCTD). At these promoters, the UP element was located at a variety of distances upstream of the CRP-binding site, which was fixed at position -41.5 bp upstream of the transcript start. At some positions, the UP element caused enhanced promoter activity whereas, at other positions, it had very little effect. In no case was the CRP-dependence of the promoter relieved. DNase I and hydroxyl-radical footprinting were used to study ternary RNA polymerase-CRP-promoter complexes formed at two of the most active of these promoters, and co-operativity between the binding of CRP and purified α subunits was studied. The footprints show that αCTD binds to the UP element as it is displaced upstream but that this displacement does not prevent αCTD from being contacted by CRP. Models to account for this are discussed.


2017 ◽  
Vol 55 (10) ◽  
pp. 816-822
Author(s):  
Matt N. Hicks ◽  
Sanjiva Gunasekara ◽  
Jose Serate ◽  
Jin Park ◽  
Pegah Mosharaf ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document